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Tramadol/APAP

NDC 72189-671 · Direct_rx

Generic nameTramadol/APAP
Dosage formTABLET
RouteORAL
Active ingredient(s)ACETAMINOPHEN, TRAMADOL HYDROCHLORIDE
Strength325; 37.5 mg/1; mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCIV
Marketing categoryANDA

Packages

72189-671-60 — 60 TABLET in 1 BOTTLE (72189-671-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72189-382 — Tramadol Hydrochloride and Acetaminophen, 72189-397 — Oxycodone/APAP, 72189-399 — Hydrocodone/APAP, 72189-406 — HYDROCODONE/APAP, 72189-407 — Hydrocodone/APAP, 72189-441 — Butal/APAP/Caff, 72189-521 — Tramadol HCL ER, 72189-600 — BUTAL/APAP/CAFFEINE, 72189-649 — Hydrocodone/APAP, 72189-650 — Hydrocodone/APAP, 72245-193 — oxycodone and acetaminophen, 72245-648 — oxycodone hydrochloride and acetaminophen, 72245-681 — oxycodone and acetaminophen, 72245-682 — oxycodone and acetaminophen, 72245-683 — oxycodone and acetaminophen, 72260-129 — ACETAMINOPHEN and IBUPROFEN, 72288-008 — Acetaminophen, 72288-056 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 72288-105 — Acetaminophen, 72288-117 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, +3602 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.